Modeling the behavior of monoclonal antibodies on hydrophobic interaction chromatography resins

Douglas Nolan , Thomas R. Chin , Mick Eamsureya , Sheldon Oppenheim , Olga Paley , Christina Alves , George Parks

Bioresources and Bioprocessing ›› 2024, Vol. 11 ›› Issue (1) : 25

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Bioresources and Bioprocessing ›› 2024, Vol. 11 ›› Issue (1) : 25 DOI: 10.1186/s40643-024-00738-8
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Modeling the behavior of monoclonal antibodies on hydrophobic interaction chromatography resins

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Abstract

Monoclonal antibodies (mAbs) require a high level of purity for regulatory approval and safe administration. High-molecular weight (HMW) species are a common impurity associated with mAb therapies. Hydrophobic interaction chromatography (HIC) resins are often used to remove these HMW impurities. Determination of a suitable HIC resin can be a time and resource-intensive process. In this study, we modeled the chromatographic behavior of seven mAbs across 13 HIC resins using measurements of surface hydrophobicity, surface charge, and thermal stability for mAbs, and hydrophobicity and zeta-potential for HIC resins with high fit quality (adjusted R 2 > 0.80). We identified zeta-potential as a novel key modeling parameter. When using these models to select a HIC resin for HMW clearance of a test mAb, we were able to achieve 60% HMW clearance and 89% recovery. These models can be used to expedite the downstream process development for mAbs in an industry setting.

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Bioprocess engineering / Chromatography / Statistical analysis / Bioengineering

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Douglas Nolan, Thomas R. Chin, Mick Eamsureya, Sheldon Oppenheim, Olga Paley, Christina Alves, George Parks. Modeling the behavior of monoclonal antibodies on hydrophobic interaction chromatography resins. Bioresources and Bioprocessing, 2024, 11(1): 25 DOI:10.1186/s40643-024-00738-8

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Funding

Takeda Pharmaceuticals U.S.A.

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